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136511-43-8

136511-43-8 Structure

136511-43-8 Structure
IdentificationBack Directory
[Name]

SCH 42495
[CAS]

136511-43-8
[Synonyms]

SCH 42495
ETHYL N-{2-[(ACETYLTHIO)METHYL]-3-(O-TOLYL)-1-OXOPROPYL}-L-METHIONATE
N-(2(S)-(Acetylthiomethyl)-3-(2-Methylphenyl)-1- Oxopropyl)-L-Methionine Ethyl Ester
L-Methionine, N-[(2S)-2-[(acetylthio)methyl]-3-(2-methylphenyl)-1-oxopropyl]-, ethyl ester
[Molecular Formula]

C20H29NO4S2
[MOL File]

136511-43-8.mol
[Molecular Weight]

411.58
Chemical PropertiesBack Directory
[Boiling point ]

597.3±50.0 °C(Predicted)
[density ]

1.158±0.06 g/cm3(Predicted)
[pka]

13.50±0.46(Predicted)
Hazard InformationBack Directory
[Uses]

SCH 42495 is an orally active neutral metalloendopeptidase (NEP) inhibitor with antihypertensive effect. SCH 42495 is the orally active ethylester proagent of SCH 42354[1].
[in vivo]

SCH 42495 (30 mg/kg; oral gavage; twice daily) causes a significant reduction in the pulmonary vascular remodelling and ventricular hypertrophy in hypoxic rats after 10 days[2].
Treatment with SCH 42495 (30 mg/kg; oral gavage; twice daily) leads to a decrease in cardiovascular remodelling secondary to chronic hypoxia in rats[2].
SCH 42495 (oral doses of 1, 3, or 10 mg/kg) produces significant reductions in blood pressure in DOCA-N a hypertensive rats of 22±6, 43±7, and 62±12 mm Hg, respectively[1].

Animal Model:Hypoxic rats[2]
Dosage:30 mg/kg
Administration:Oral gavage; twice daily for 10 days
Result:Caused a significant reduction in the pulmonary vascular remodelling and ventricular hypertrophy.
Led to a decrease in cardiovascular remodelling secondary to chronic hypoxia.
[References]

[1] Watkins RW, et al. Atrial natriuretic factor potentiating and hemodynamic effects of SCH 42495, a new, neutral metalloendopeptidase inhibitor. Am J Hypertens. 1993 May;6(5 Pt 1):357-68. DOI:10.1093/ajh/6.5.357
[2] Thompson JS, et al. Effects of the neutral endopeptidase inhibitor, SCH 42495, on the cardiovascular remodelling secondary to chronic hypoxia in rats. Clin Sci (Lond). 1994 Jul;87(1):109-14. DOI:10.1042/cs0870109
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